iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs582142	snp	A/G	0.219049	0.248077	intron-variant	RNF212	GRCh38.p7	4:1095185	TGATGAGCCAGGTGC[A/G]CTATCCCGAGACCAT	285498
rs582202	snp	C/T	0.334642	0.235236	intron-variant	RNF212	GRCh38.p7	4:1095155	TGGAGCTGTGGGGGG[C/T]GTGCTTGGTTCTGTG	285498
rs583100	snp	A/G	0.290977	0.246619	intron-variant	RNF212	GRCh38.p7	4:1088398	gccaggtcacatctt[A/G]aacgctttgctgctt	285498
rs584472	snp	C/G	0.285257	0.247501	intron-variant	RNF212	GRCh38.p7	4:1094686	CAGGGCCTTCTGCCT[C/G]CCAGGCCTCCAATCC	285498
rs585735	snp	C/G	0.350546	0.22889	intron-variant	RNF212	GRCh38.p7	4:1086603	CTCACCCCCACCCCT[C/G]TCCTGCCACCCTCAT	285498
rs588824	snp	A/G	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1099171	ACATTGCAGAGGGCC[A/G]GCGATAAGCCAGGTG	285498
rs589660	snp	G/T	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1099312	CTAACAGCCCAGCAC[G/T]AAAATAAATAATAAA	285498
rs590118	snp	A/G	0.0364509	0.129988	intron-variant	RNF212	GRCh38.p7	4:1099437	TCTAAGTGAGTATTA[A/G]CTGTCCATGGCAGCA	285498
rs604526	snp	C/T	0.281841	0.247964	intron-variant	RNF212	GRCh38.p7	4:1092499	GCCTCATGCCGCCTC[C/T]GTGGTTTGTCTGGCC	285498
rs604597	snp	A/G	0.348134	0.229934	intron-variant	RNF212	GRCh38.p7	4:1100363	ACTTCCGAGCTACTG[A/G]TGCACCTGTTACATT	285498
rs606293	snp	A/G	0.291493	0.246533	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092880	GAGGCCAGGAGAGGC[A/G]GCTGCCTGGTCCGGA	285498
rs606327	snp	A/G	0.292266	0.246401	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092914	CACTTCTCACTCTTC[A/G]GTTCAATACCAGTTC	285498
rs608066	snp	A/G	0.29175	0.246489	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093278	gggttttatctgttg[A/G]tatttaccctattag	285498
rs610218	snp	C/G	0.346811	0.230494	intron-variant	RNF212	GRCh38.p7	4:1086295	TGTGCCGTGGGATGA[C/G]CTGGCAGTGGCCGTG	285498
rs614945	snp	G/T	0.17481	0.238425	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093829	CCAGCCAGAGGCCCA[G/T]GGAAACACCATCCAG	285498
rs615381	snp	A/G	0.176993	0.239102	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093743	AGTCCCCTTGGGGCC[A/G]GAAGTTGCTTGAGTT	285498
rs616196	snp	A/C	0.170523	0.23703	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093605	AGCAGACCCGGCCAG[A/C]CCCTCCAGCCACCTG	285498
rs616569	snp	C/T	0.292008	0.246445	intron-variant	RNF212	GRCh38.p7	4:1100126	AAAAGAAGATGAAAT[C/T]AGTGTTGACAGCCGA	285498
rs617633	snp	C/T	0.274393	0.248807	intron-variant	RNF212	GRCh38.p7	4:1084092	ATGTGTTGGTGCACA[C/T]CTGTAATCCCAGCTA	285498
rs619407	snp	C/G	0.290718	0.246662	intron-variant	RNF212	GRCh38.p7	4:1099470	CTGGCTCTCACTGCA[C/G]GAGGCCCCACCATAC	285498
rs620398	snp	A/G	0.291493	0.246533	intron-variant	RNF212	GRCh38.p7	4:1099232	TTCACAGACTTCAGA[A/G]TTCTTTGTTGAAAGT	285498
rs629260	snp	C/T	0.347914	0.230028	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092976	TGGTCCTGGCGTAGT[C/T]TGGAGCTCATGTGGA	285498
rs629261	snp	G/T	0.347914	0.230028	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092975	GGTCCTGGCGTAGTT[G/T]GGAGCTCATGTGGAC	285498
rs629638	snp	C/G	0.292266	0.246401	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092926	CTCCATGGAGGAGAA[C/G]TGGTATTGAACCGAA	285498
rs630549	snp	A/G	0.292266	0.246401	intron-variant	RNF212	GRCh38.p7	4:1092715	CTGACCTGGCCCAGC[A/G]CAGCCTCTGTGACCA	285498
rs632319	snp	A/G	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1098839	ACAGTGACAGTTCCC[A/G]CTCCCTGCGCACTCA	285498
rs633087	snp	A/G	0.291493	0.246533	intron-variant	RNF212	GRCh38.p7	4:1098720	TTCTGTTTTATACGT[A/G]GGGAGACCGAGGCAT	285498
rs633141	snp	A/G	0.291493	0.246533	intron-variant	RNF212	GRCh38.p7	4:1098690	TGGTGGAGTTAGGTG[A/G]AGAACCAGGGTTGCA	285498
rs633556	snp	C/T	0.398534	0.201091	intron-variant	RNF212	GRCh38.p7	4:1098617	TCCTGATGCCTGTGG[C/T]GTTGGACATACTGCT	285498
rs633599	snp	A/G	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1098576	CAGTTTGGTGTGTAT[A/G]GGAGGGTGTTACACG	285498
rs633954	snp	C/T	0.292008	0.246445	intron-variant	RNF212	GRCh38.p7	4:1094484	AGAGAATGGACAAGC[C/T]GCAACTGAGAGGACT	285498
rs636976	snp	A/G	0.291493	0.246533	intron-variant	RNF212	GRCh38.p7	4:1095127	TGGTCTCAGGATAGC[A/G]CACCTGGCTCATCAC	285498
rs641987	snp	A/G	0.350327	0.228986	intron-variant	RNF212	GRCh38.p7	4:1083754	GCTGTGATCTCCGTC[A/G]TCTTAGGCCACCTGG	285498
rs643043	snp	A/G	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1092146	ACATGTGAAGCTGAG[A/G]AGCAGAGGCGCTTGC	285498
rs643484	snp	C/T	0.347032	0.230401	intron-variant	RNF212	GRCh38.p7	4:1092038	GGCGTGTGCAGGTGT[C/T]CCCGACAGGCAGCAG	285498
rs646117	snp	C/G	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1098041	GTCTTGCTCTGTTGC[C/G]CAGGCTGGAGTGCAG	285498
rs647828	snp	C/G	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1097702	CTAATGTGGTCCTGG[C/G]TGGGGAAAGTGAGGG	285498
rs648640	snp	A/G	0.0208471	0.0999448	intron-variant	RNF212	GRCh38.p7	4:1096714	GCTCCATGGTCTCGG[A/G]ATAGTGCACCTGGCT	285498
rs649243	snp	A/G	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1090977	GCACTGGCCATGGGC[A/G]TCTGTGGGGGCAGGA	285498
rs649258	snp	A/G	0.295599	0.245806	intron-variant	RNF212	GRCh38.p7	4:1097375	ccttgtgatccgccc[A/G]cctcggcctcccaaa	285498
rs649616	snp	A/G	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1097319	ccgctcccgaccTAC[A/G]AGACGCTGTTTCTTA	285498
rs649950	snp	A/G	0.278399	0.248382	intron-variant	RNF212	GRCh38.p7	4:1096998	GCCAGGGACAGCCTC[A/G]ATCAACAGGACAGCC	285498
rs651017	snp	A/G	0.401037	0.199218	intron-variant	RNF212	GRCh38.p7	4:1097274	TTATTTAAAAAGCAA[A/G]TGTAAGGACCTTAAG	285498
rs651135	snp	C/T	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1090543	GCATGGGCCTCCCTG[C/T]CTGGCCACACTTATC	285498
rs651509	snp	C/T	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1090515	ATCCCCTCAGCCACC[C/T]GGGGCAACACTGGGG	285498
rs652063	snp	A/G	0.347253	0.230308	intron-variant	RNF212	GRCh38.p7	4:1090349	TGGGGCCGCTTCCCC[A/G]AGTCTGGAAGCCAGC	285498
rs658320	snp	C/T	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1091059	GAATGGAGCAGGTTG[C/T]TGGGGAGACTTTCCT	285498
rs658846	snp	C/G	0.27223	0.24966	intron-variant	RNF212	GRCh38.p7	4:1090935	CAAGCACTGTGAGCT[C/G]TCCTGAGAGTCCCTC	285498
rs661364	snp	G/T	0.292951	0.250548	intron-variant	RNF212	GRCh38.p7	4:1096974	CCCTGGCAGGGCCCC[G/T]GAGAGGCCATTCACA	285498
rs662667	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1096697	CGAGACCATGGAGCT[A/G]TGAGGGGTGTGCTTG	285498
rs662731	snp	A/G	0.208353	0.246507	intron-variant	RNF212	GRCh38.p7	4:1096635	GACCATGGAGCTGTG[A/G]GGGGTGTGCTTGGTT	285498
rs662732	snp	A/G	0.208353	0.246507	intron-variant	RNF212	GRCh38.p7	4:1096633	CCATGGAGCTGTGAG[A/G]GGTGTGCTTGGTTCT	285498
rs671790	snp	C/G	0.268724	0.249298	intron-variant	RNF212	GRCh38.p7	4:1083097	CTCTCTACATACCTG[C/G]TATCGCCTGCATTTT	285498
rs674347	snp	A/G	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1089797	TAACAGCAGGAGAGA[A/G]GGCAGGGGGAACTGC	285498
rs676561	snp	A/G	0.347694	0.230122	intron-variant	RNF212	GRCh38.p7	4:1089324	ccccatgcaagtcca[A/G]aacccagcagggcag	285498
rs681857	snp	A/G	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1098137	AATGACAAGATGTAG[A/G]AAGAACCTCATGCCT	285498
rs682243	snp	A/G	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1098198	GCATAGAGTCAAGAC[A/G]GTCATCTAAGCCCAT	285498
rs682787	snp	C/T	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1098370	TGGCTTGGATCAGGA[C/T]TAAGGCACCAGCTCC	285498
rs687939	snp	G/T	0.29175	0.246489	intron-variant	RNF212	GRCh38.p7	4:1089087	ggcgtctggaggaca[G/T]tggccctcttctcat	285498
rs688008	snp	A/G	0.347694	0.230122	intron-variant	RNF212	GRCh38.p7	4:1089041	caccccagttgggac[A/G]ctgtgtgggaacaac	285498
rs688785	snp	C/G	0.347473	0.230215	intron-variant	RNF212	GRCh38.p7	4:1088919	ttccatacatcttct[C/G]aaatctaggtggagg	285498
rs689216	snp	A/T	0.292008	0.246445	intron-variant	RNF212	GRCh38.p7	4:1088825	atgcttggggtttgc[A/T]ccctctgaagcagca	285498
rs935968	snp	A/C	0.405603	0.195673	intron-variant	RNF212	GRCh38.p7	4:1069399	TACCTTTTGCCTCAT[A/C]CGGCCTCACCCCCCA	285498
rs935969	snp	C/T	0.366473	0.221211	intron-variant	RNF212	GRCh38.p7	4:1068800	ccaatgaaattaaca[C/T]tttaaaatgaagact	285498
rs1010342	snp	A/G	0.367091	0.220884	intron-variant	RNF212	GRCh38.p7	4:1075031	AAATCTCCGCAGAGC[A/G]TTCAAGTGCTGGTGT	285498
rs1383660	snp	C/T	0.293294	0.246223	intron-variant	RNF212	GRCh38.p7	4:1107428	TCCTGGTCACTGTCA[C/T]CTCTGGGAAACAGGA	285498
rs1453605	snp	A/G	0.499575	0.0145705	intron-variant	RNF212	GRCh38.p7	4:1081983	GATGATGGACATGAG[A/G]CACCATGGCTGGCCT	285498
rs1466214	snp	A/G	0.481242	0.0950111	intron-variant	RNF212	GRCh38.p7	4:1079972	AGGGAGAAGCTGAGT[A/G]TGCAGAGGTGCAAGA	285498
rs1466215	snp	A/G	0.49889	0.0235361	intron-variant	RNF212	GRCh38.p7	4:1078432	CCGTCGTCTGTCCTG[A/G]TGGGCAGAACTCAGC	285498
rs1466216	snp	C/T	0.440609	0.161766	intron-variant	RNF212	GRCh38.p7	4:1078119	AGCCCTTTATAGATA[C/T]GAACTCAGTCGTGTA	285498
rs1670533	snp	C/T	0.350546	0.22889	RNF212	4	allele_origin=T(germline)/C(germline)	4:1084399	ATGGCTTTTACATTT[C/T]TAGAAGATTGTAAAC	285498
rs1670534	snp	A/G	0.375258	0.216357	intron-variant, missense	RNF212	GRCh38.p7	4:1093477	ACTGTGGAGGTGAGC[A/G]TCACAAACGCAGGGT	285498
rs1680026	snp	A/G	0.292523	0.246357	intron-variant	RNF212	GRCh38.p7	4:1092801	GCGAACTGGGAGGCC[A/G]AGAAGGCCTGAGAGT	285498
rs1680027	snp	A/C	0.292523	0.246357	intron-variant	RNF212	GRCh38.p7	4:1092802	CGAACTGGGAGGCCG[A/C]GAAGGCCTGAGAGTC	285498
rs1825092	snp	A/G	0.292523	0.246357	intron-variant	RNF212	GRCh38.p7	4:1107121	cagtggtgtgatctc[A/G]gctcaccacagcctc	285498
rs1825093	snp	A/G	0.49614	0.0437598	intron-variant	RNF212	GRCh38.p7	4:1107294	ctgacctcatgatcc[A/G]cctgcctcagcctcc	285498
rs2014318	snp	A/G	0.349671	0.229272	intron-variant	RNF212	GRCh38.p7	4:1074990	GTCCCTTCGAACTAC[A/G]TTCCATTTGCTGCTC	285498
rs2045065	snp	C/T	0.347032	0.230401	intron-variant	RNF212	GRCh38.p7	4:1058700	TTGCTATCCAGCTGC[C/T]GATGATTCAGATGGC	285498
rs2045066	snp	A/G	0.361894	0.223562	intron-variant	RNF212	GRCh38.p7	4:1058613	TATTTACGCCCTCAT[A/G]TGGAAGACCCAGGGC	285498
rs2045067	snp	A/G	0.350327	0.228986	intron-variant	RNF212	GRCh38.p7	4:1058567	GTTGGCACCAGGGCT[A/G]CCCGCAACCTAAGAG	285498
rs2045068	snp	C/T	0.349452	0.229367	intron-variant	RNF212	GRCh38.p7	4:1058424	ATGTGTTAACATGAA[C/T]GACTCATGTTTTATT	285498
rs2045069	snp	A/G	0.349671	0.229272	intron-variant	RNF212	GRCh38.p7	4:1058418	TAACATGAACGACTC[A/G]TGTTTTATTCTTGTT	285498
rs2100411	snp	A/G	0.350109	0.229081	intron-variant	RNF212	GRCh38.p7	4:1080624	ggcaggtttcccgtg[A/G]ggagttttaattggt	285498
rs2248083	snp	G/T	0.346811	0.230494	missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1058378	GCAGCGTCTCCTCCC[G/T]GGGCCCCGAGCATCC	285498
rs2290407	snp	A/G	0.254498	0.24996	intron-variant	RNF212	GRCh38.p7	4:1081483	GACGCTGGCATTTTC[A/G]TCATCACTCTTCCAG	285498
rs2290408	snp	A/C	0.347473	0.230215	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073479	TGCTGTCCTTCCACC[A/C]GGTGCATGGGAGGCT	285498
rs2290409	snp	A/G	0.498813	0.0243321	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073461	TGCATGGGAGGCTAC[A/G]TATTCACCAAAATGG	285498
rs2290410	snp	A/T	0.363776	0.222609	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058290	AAGCACCTTCTTCAC[A/T]GCGTTCTAACCCCCG	285498
rs2290411	snp	A/G	0.350982	0.228698	intron-variant	RNF212	GRCh38.p7	4:1057289	GCTTTTGATGCCTGC[A/G]GTCCAGTCCACCCCT	285498
rs2924495	snp	C/T	0.291235	0.246576	intron-variant	RNF212	GRCh38.p7	4:1097713	AGTGTTTTGTGCTAA[C/T]GTGGTCCTGGCTGGG	285498
rs2932768	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1067806	ccaggagtcggaggt[A/T]gcagtgagccgagat	285498
rs3199881	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1101018	GAAATTACAGACAGG[A/G]GTTTTAACATTGTGG	285498
rs3221827	microsatellite	(CA)11/12/17/18/19/20/21/22	0.786708	0.124735	intron-variant	RNF212	GRCh38.p7	4:1106251	AAACAATTTTACTTA[(CA)11/12/17/18/19/20/21/22]AGTCACTCAGACACA	285498
rs3796619	snp	C/T	0.498982	0.0225409	RNF212	4	allele_origin=T(germline)/C(germline)	4:1101493	CAGGTGGCAGAGTCA[C/T]AATCCTTCAACAGGA	285498
rs3796620	snp	C/T	0.350546	0.22889	intron-variant	RNF212	GRCh38.p7	4:1101291	AAAACAATACAATTA[C/T]GGAAAATCAGTGAAA	285498
rs3816474	snp	C/T	0.275197	0.248727	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056865	CCGCCCATCAGCATC[C/T]CCAGCCTGCTGCAGA	285498
rs4045481	snp	A/G	0.46341	0.130216	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1096837	CTGGATATCTGCGTC[A/G]GTCTGAAAGAGAAAG	285498
rs4045482	in-del	-/GA			intron-variant	RNF212	GRCh38.p7	4:1098189	CAGTGAGCGCATAGA[-/GA]GTCAAGACGGTCATC	285498
rs4246683	snp	A/G	0.293037	0.246268	intron-variant	RNF212	GRCh38.p7	4:1110215	CTCACTAGTCAATTA[A/G]AAAGAAACACCTCAA	285498
rs4246684	snp	A/G	0.293294	0.246223	intron-variant	RNF212	GRCh38.p7	4:1110416	GGTCGCATTTGGGTC[A/G]GTTTTCATGTGCACA	285498

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